Oral phenotype and variation in focal dermal hypoplasia
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference30 articles.
1. Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: The odonto-onycho-dermal dysplasia;Adaimy;Am J Hum Genet,2007
2. Enamel defects and Lyonization in focal dermal hypoplasia;Balmer;Oral Surg Oral Med Oral Pathol Oral Radiol Endod,2004
3. Deletion of mouse Porcn blocks Wnt ligand secretion and reveals an ectodermal etiology of human focal dermal hypoplasia/Goltz syndrome;Barrott;Proc Natl Acad Sci USA,2011
4. Dental and oral lesions in two patients with focal dermal hypoplasia (Goltz syndrome);Baxter;Br Dent J,2000
5. Zygotic Porcn paternal allele deletion in mice to model human focal dermal hypoplasia;Biechele;PLoS ONE,2013
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